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1-Phenyl-2-(1-piperidylimino)ethanone

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Identification
Molecular formula
C13H16N2O
CAS number
.
IUPAC name
1-phenyl-2-(1-piperidylimino)ethanone
State
State

This compound is typically found in a solid state at room temperature. The crystalline nature of the compound indicates stable solid form with a potential range of hydration levels, sometimes affecting its granularity or color intensity.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
244.32g/mol
Molar mass
244.3240g/mol
Density
1.0400g/cm3
Appearence

1-Phenyl-2-(1-piperidylimino)ethanone typically appears as a crystalline solid. The crystals are often slightly yellow to white in color, suggesting the presence of slight impurities or varying levels of hydration. Its form is typical of organic compounds having aromatic and heterocyclic moieties, where varied factors like humidity might influence its final presentation.

Comment on solubility

Solubility of 1-phenyl-2-(1-piperidylimino)ethanone

The solubility of 1-phenyl-2-(1-piperidylimino)ethanone, a compound rich in aromatic and nitrogen functionalities, can vary widely depending on the solvent used. Here are some key points regarding its solubility:

  • Polar solvents: This compound tends to demonstrate good solubility in polar solvents such as water and methanol. The presence of the piperidine ring enhances its interactions with the solvent, promoting better solubility.
  • Non-polar solvents: In contrast, 1-phenyl-2-(1-piperidylimino)ethanone may have limited solubility in non-polar solvents like hexane or cyclohexane due to its polar functional groups.
  • Temperature effects: Increasing the temperature often enhances solubility, as it provides more energetic interaction between the solvent and solute.
  • Concentration factors: Generally, higher concentrations of the compound lead to precipitation if the solvent's capacity is exceeded, showcasing the importance of saturation levels.

In summary, the solubility of 1-phenyl-2-(1-piperidylimino)ethanone is influenced by the polarity of the solvent, temperature conditions, and concentration, making it essential to choose the appropriate medium for desired applications. "Like dissolves like" is a guiding principle for understanding its solubility behavior.

Interesting facts

Interesting Facts about 1-phenyl-2-(1-piperidylimino)ethanone

1-phenyl-2-(1-piperidylimino)ethanone, often referred to in the realm of medicinal chemistry, is a fascinating compound due to its structural features and potential applications. Below are some engaging insights into this intriguing molecule:

  • Structural Diversity: The compound exhibits a unique combination of a phenyl group and a piperidine moiety, showcasing the intricate relationship between aromatic and aliphatic systems in organic chemistry.
  • Biological Activity: Researchers have shown interest in this compound for its potential biological properties, particularly in drug design and development. Compounds that incorporate piperidine structures are often explored for their pharmacological effects.
  • Synthetic Pathways: The synthesis of 1-phenyl-2-(1-piperidylimino)ethanone involves multi-step reactions that may include condensation and functional group transformations, illustrating the beauty of organic synthesis.
  • Applications in Research: Due to its structural characteristics, this compound can serve as a lead structure for developing new pharmaceuticals. Exploring its derivatives could yield novel therapeutic agents.
  • Interdisciplinary Interest: The compound garners attention across various fields including medicinal chemistry, organic synthesis, and materials science, highlighting its versatility in chemical research.

As stated in the words of a renowned chemist, "The beauty of chemistry lies in its ability to forge connections between seemingly unrelated domains." 1-phenyl-2-(1-piperidylimino)ethanone is a prime example of how a small modification in structure can lead to vast possibilities in chemical behavior and application. This compound embodies a rich intersection of organic chemistry and medicinal applications, inspiring ongoing research and interest in its study.